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Homologous Recombination02:31

Homologous Recombination

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The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
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Single-Strand DNA Binding Proteins01:03

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For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
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DNA Isolation01:24

DNA Isolation

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DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow...
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DNA Isolation01:34

DNA Isolation

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DNA from cells is required for many biotechnology and research applications, such as molecular cloning. To remove and purify DNA from cells, researchers use various methods of DNA extraction. While the specifics of different protocols may vary, some general concepts underlie the process of DNA extraction.
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DNA Topoisomerases02:02

DNA Topoisomerases

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Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
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Mismatch Repair01:20

Mismatch Repair

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Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
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The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
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Related Experiment Video

Updated: Mar 24, 2026

Methods to Increase the Sensitivity of High Resolution Melting Single Nucleotide Polymorphism Genotyping in Malaria
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Methods to Increase the Sensitivity of High Resolution Melting Single Nucleotide Polymorphism Genotyping in Malaria

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Premeltons in DNA.

Henry M Sobell1

  • 1Departments of Chemistry and Molecular Biophysics, University of Rochester, Rochester, NY, 14642, USA. sobell@localnet.com.

Journal of Structural and Functional Genomics
|March 18, 2016
PubMed
Summary

Premeltons, DNA structural solitons, explain DNA melting and transitions. These emergent structures, including beta-DNA, offer a unifying theory for DNA physical chemistry and gene regulation.

Keywords:
Actinomycin-DNA bindingB- to A- DNA structural phase-transitionDNA transcriptionDNA-melting and premeltingElongationEthidium-DNA bindingGene-regulationInitiationIntercalationMeltonsPremeltonsProtein: DNA allosterismRNA-polymerase: promoter recognitionTermination of RNA-synthesis

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Area of Science:

  • Molecular Biology
  • Biophysics
  • Structural Biology

Background:

  • DNA exhibits complex structural dynamics beyond the canonical B- and A-forms.
  • Nonlinear excitations are proposed to drive emergent structures within DNA.
  • Understanding these structures is crucial for DNA physical chemistry and molecular biology.

Purpose of the Study:

  • To introduce and elaborate on the concept of premeltons as emergent DNA structures.
  • To explain the two types of premeltons (B-B/A-A and B-A/A-B) and their properties.
  • To present a unifying theoretical model for DNA physical chemistry and gene structure based on premeltons.

Main Methods:

  • Theoretical modeling of DNA nonlinear dynamics.
  • Analysis of structural-soliton properties (premeltons).
  • Characterization of the intermediate beta-DNA structure.

Main Results:

  • Identified two types of premeltons: stationary (B-B/A-A) and mobile (B-A/A-B).
  • Described beta-DNA as a metastable, hyperflexible intermediate structure with unique sugar-puckering and base-stacking.
  • Proposed premeltons define gene boundaries (5' and 3' ends) in DNA.

Conclusions:

  • Premeltons provide a unifying framework for understanding DNA melting, structural transitions, and gene organization.
  • The model predicts premeltons' role in regulating transcription initiation, elongation, and termination.
  • The theory offers testable experimental predictions for DNA physical chemistry and molecular biology.